Device recall
Z-2137-2011: NX is the radiographer's image identification and quality control tool. It…
FDA device recall · Class II · AGFA Corp.
Key facts
| Recall number (Z-number) | Z-2137-2011 |
|---|---|
| Recall event | 58166 |
| Product | NX is the radiographer's image identification and quality control tool. It offers a broad array of features developed especially to meet the needs of the radiographer. Standard tasks are completed quickly and effortlessly with a simple touch screen. In-room integration provides a more convenient… |
| Product code | MQB |
| Recalling firm | AGFA Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2012 |
| 510(k) numbers | K071162 |
| FEI number | 3001236302 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database